Welcome to LookChem.com Sign In|Join Free

CAS

  • or

22445-93-8

Post Buying Request

22445-93-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

22445-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22445-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,4 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22445-93:
(7*2)+(6*2)+(5*4)+(4*4)+(3*5)+(2*9)+(1*3)=98
98 % 10 = 8
So 22445-93-8 is a valid CAS Registry Number.

22445-93-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,7-dimethyl-6-azaspiro[4.5]decan-9-one

1.2 Other means of identification

Product number -
Other names 6-Aza-7,7-dimethyl-spiro<4.5>decan-9-on

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22445-93-8 SDS

22445-93-8Downstream Products

22445-93-8Relevant articles and documents

Oxoammonium Salts. 5. A New Synthesis of Hindered Piperidines Leading to Unsymmetrical TEMPO-Type Nitroxides. Synthesis and Enantioselective Oxidations with Chiral Nitroxides and Chiral Oxoammonium Salts

Ma, Zhenkun,Huang, Qingtao,Bobbitt, James M.

, p. 4837 - 4843 (2007/10/02)

A new synthesis of unsymmetrical 2,2,6,6-tetraalkyl-4-piperidones from acetonin (2,2,4,4,6-pentamethyl-2,3,4,5-tetrahydropyrimidine) and several ketones is described.When the ketone was a naturally occurring optically active ketone, the piperidones were optically active.The piperidones were converted to unsymmetrical TEMPO-type nitroxides and chiral nitroxides.The optically active nitroxides were used as catalysts for oxidations or converted to chiral oxoammonium salts.The structures of the chiral compounds were determined by 2D (1)H and (13)C NMR, and the cyclic voltammetric properties of the various nitroxides were measured.Several other pyrrolidine oxoammonium salts were prepared, and both types were used as oxidizing agents.Preliminary results of chiral oxidations are presented.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 22445-93-8